{3-[4-(8-Benzyloxy-imidazo[1,2-a]pyridin-2-yl)-phenoxy]-propyl}-dibutyl-amine | 114604-59-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: {3-[4-(8-Benzyloxy-imidazo[1,2-a]pyridin-2-yl)-phenoxy]-propyl}-dibutyl-amine
• 英文别名: N-butyl-N-[3-[4-(8-phenylmethoxyimidazo[1,2-a]pyridin-2-yl)phenoxy]propyl]butan-1-amine
• CAS: 114604-59-0
• 化学式: C₃₁H₃₉N₃O₂
• 分子量: 485.67
• InChiKey: ZKUYPDDYTXCSNB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.8
• 重原子数：
  36
• 可旋转键数：
  15
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  39
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-bromo-1-(4-(3-chloropropoxy)phenyl)ethanone 以 乙醇 为溶剂， 反应 24.0h， 生成 {3-[4-(8-Benzyloxy-imidazo[1,2-a]pyridin-2-yl)-phenoxy]-propyl}-dibutyl-amine
  参考文献：
  名称：

  Synthesis of (aryloxy)alkylamines. 2. Novel imidazo-fused heterocycles with calcium channel blocking and local anesthetic activity

  摘要：

  A series of imidazo-fused heterocycles substituted with an aryloxy)alkylamine side chain were prepared as modifications to butoprozine (I) and found to possess calcium channel blocking activity similar in potency to that of bepridil in trachea smooth muscle and similar to that of verapamil in nitrendipine binding affinity in rabbit cardiac muscle. Of the various imidazo-fused heterocycles prepared, the imidazo[1,2-a]pyridines were also found to be potent local anesthetic agents. While most compounds in this series were equipotent to lidocaine in our initial screen, compounds 2 and 35 showed local anesthetic activity approximately 100 times more potent than lidocaine in our preliminary assays. These compounds represent a novel structural class of local anesthetic agents, and compound 2 is under further investigation.

  DOI：

  10.1021/jm00119a026

文献信息

• 2- or 3- Aryl substituted imidazo [1,2-a] pyridines
  申请人：ORTHO PHARMACEUTICAL CORPORATION

  公开号：EP0261912A2

  公开（公告）日：1988-03-30

  Novel 2- or 3- aryl substituted imidazo[1,2-a]pyridines and their synthesis are described. The compounds have local anesthetic properties and are useful as local anesthetic agents, calcium channel blocking agents and antisecretory acents.

  介绍了新型 2-或 3-芳基取代咪唑并[1,2-a]吡啶及其合成方法，这些化合物具有局部麻醉特性，可用作局部麻醉剂、钙通道阻滞剂和抗分泌剂。
• PRESS, JEFFERY B.
  作者：PRESS, JEFFERY B.

  DOI：——

  日期：——
• US4727145A
  申请人：——

  公开号：US4727145A

  公开（公告）日：1988-02-23
• US4791117A
  申请人：——

  公开号：US4791117A

  公开（公告）日：1988-12-13
• US4871745A
  申请人：——

  公开号：US4871745A

  公开（公告）日：1989-10-03